Explore the Potential with AI-Driven Innovation
The focused library is created on demand with the latest virtual screening and parameter assessment technology, supported by the Receptor.AI drug discovery platform. This method is more effective than traditional methods and results in higher-quality compounds with better activity, selectivity, and safety.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner Reaxense.
Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.
Our high-tech, dedicated method is applied to construct targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
By deploying molecular simulations, our approach comprehensively covers a broad array of proteins, tracking their flexibility and dynamics individually and within complexes. Ensemble virtual screening is utilised to take into account conformational dynamics, identifying pivotal binding sites located within functional regions and at allosteric locations. This thorough exploration ensures that every conceivable mechanism of action is considered, aiming to identify new therapeutic targets and advance lead compounds throughout a vast spectrum of biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
P63104
UPID:
1433Z_HUMAN
Alternative names:
Protein kinase C inhibitor protein 1
Alternative UPACC:
P63104; A8K1N0; B7Z465; P29213; P29312; Q32P43; Q5XJ08; Q6GPI2; Q6IN74; Q6NUR9; Q6P3U9; Q86V33
Background:
The 14-3-3 protein zeta/delta, also known as Protein kinase C inhibitor protein 1, plays a pivotal role in cellular processes by acting as an adapter protein. It regulates a broad spectrum of signaling pathways by binding to partners through phosphoserine or phosphothreonine motifs, modulating their activity. This protein is crucial in maintaining cytosolic retention and inactivation of TFEB transcription factor, enhancing ARHGEF7 activity on RAC1, and is involved in the formation of lamellipodia and membrane ruffles. In neuronal contexts, it is essential for spine maturation by modulating ARHGEF7 activity.
Therapeutic significance:
Understanding the role of 14-3-3 protein zeta/delta could open doors to potential therapeutic strategies.